Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Crossroads is recalling 2016-2017 Z1 Lite travel trailers because a furnace exhaust cover may mislabel the hot tube location, posing burn and fire risks.
Philips is recalling actuator assemblies for angiographic x-ray monitor ceiling suspension systems because the actuator can detach, causing the monitor carriage to drop.
Nihon Kohden America Inc is recalling MEE-1000A Neuromaster accessories due to defective printed circuit boards that failed to prevent unintentional current flow.
ViewRay is recalling five MRIdian Radiation Therapy Systems because they loaded a completion fraction in the incorrect order after a treatment interruption.
CareFusion 303, Inc. is recalling 9,345 Jadak Barcode Scanners used with Pyxis Anesthesia systems because they may transmit incorrect medication information to the dispensing system.
Kwik Trip Bakery is recalling Cinnamon Crunch Bagels because they may contain pieces of plastic from contaminated ice nuggets used as an ingredient.
Isuzu is recalling certain 2016 NPR-HD, NPR-XD, NQR, and NRR trucks because typographical errors on the certification label may prevent accurate vehicle loading and maintenance.
Kwik Trip Bakery is recalling fresh glazed donuts that may contain pieces of plastic due to contaminated ice nuggets used as an ingredient.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including progesterone/testosterone, due to lack of sterility assurance found during an FDA inspection.
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine prostaglandin, after FDA inspection found lack of sterility assurance.
Daimler Trucks North America is recalling 2012-2017 Thomas Built Buses Minotour school buses because a body control module failure may cause loss of exterior lighting or windshield wipers.
Daimler Vans USA is recalling 2015-2016 Sprinter vans because tire pressure labels list incorrect maximum load capacities, which could lead to axle or tire failure.
Apple is recalling approximately 814,000 travel adapter kits and plug adapters because the two-prong adapters can break and expose metal, posing an electric shock risk.
ENVE is recalling about 600 carbon fiber bicycle forks because the left leg can crack, posing a fall hazard. No injuries have been reported.
Evenflo is recalling specific Transitions 3-in-1 Combination Booster Seats because the harness adjuster button may be within a child's reach, allowing them to loosen the harness and increasing injury risk in a crash.
Raynor Marketing is recalling about 1,200 Eurotech Lume office chairs because the seat can detach, posing a fall hazard. No injuries have been reported.
BYA Sports is recalling Skyline backyard zipline kits because a cable crimp can fail, posing a fall hazard. Consumers should stop using the kits and contact the company for a free replacement.
Boa is recalling snowboard boots with M3v2 secondary reels because the mechanism can get stuck, loosening the fit and posing a fall hazard. No injuries have been reported.
J. Crew is recalling specific girls' puffer coats because front buttons can detach, posing a choking hazard to young children. No injuries have been reported.
Forest River is recalling 2016 Coachmen Galleria motorhomes because the Federal Placards incorrectly list seatbelts and omit the Gross Vehicle Weight Rating, increasing crash risk.
Navistar is recalling 2016-2017 IC CE school buses because hood straps may elongate, allowing the hood to open unexpectedly during braking and obstructing the driver's vision.
Orthofix is recalling 36 Firebird Spinal Fixation System Torque Limiting Handles because they may deliver less torque than required after sterilization, potentially causing spinal construct loosening.
Macleods Pharma USA is recalling Pramipexole Dihydrochloride tablets due to the presence of a foreign Carbimazole 5 mg tablet.
Kraft Heinz is recalling Kraft Singles White American cheese slices because packaging film may remain on the slice, posing a choking risk.
Philips is recalling TraumaDiagnost radiological examination units because the arm may not be fastened securely and could fall down.